| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39330229-39330260 | Rare:8 | ||||
| chr3:39383227-39383474 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383476-39383732 | Common:1; Rare:61; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:39406414-39406823 | Common:7; Rare:156 | ||||
| chr3:39406926-39407139 | Common:5; Rare:80 | ||||
| chr3:40309406-40309890 | Common:9; Rare:154 | ||||
| chr3:40310345-40310393 | Rare:9 | ||||
| chr3:40457082-40457452 | Common:7; Rare:140 | ||||
| chr3:40457540-40457611 | Rare:23 | ||||
| chr3:40477020-40477260 | Common:2; Rare:58 | ||||
| chr3:40505846-40506208 | Rare:87 | ||||
| chr3:40506248-40506403 | Rare:44 | ||||
| chr3:40524684-40525183 | Common:2; Rare:125 | ||||
| chr3:41199267-41199627 | Common:1; Rare:155 | ||||
| chr3:41199902-41200158 | Common:1; Rare:67 |